(4S,4'S)-2,2'-(1,3-Di(quinolin-2-yl)propane-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole)

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Reagent Code: #236884
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CAS Number 2490297-23-7

science Other reagents with same CAS 2490297-23-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 616.75 g/mol
Formula C₄₁H₃₆N₄O₂
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid oxazoline-quinoline framework coordinates effectively with transition metals like copper or palladium, enabling high stereocontrol in reactions such as cyclopropanations, aldol additions, and allylic alkylations. The ligand’s C2-symmetry and steric bulk enhance enantioselectivity, making it valuable in the synthesis of pharmaceuticals and fine chemicals where precise chirality is critical. It is especially effective in reactions requiring mild conditions and high yield with minimal byproduct formation.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,980.00
inventory 250mg
10-20 days ฿7,420.00
inventory 1g
10-20 days ฿25,590.00

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(4S,4'S)-2,2'-(1,3-Di(quinolin-2-yl)propane-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole)
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid oxazoline-quinoline framework coordinates effectively with transition metals like copper or palladium, enabling high stereocontrol in reactions such as cyclopropanations, aldol additions, and allylic alkylations. The ligand’s C2-symmetry and steric bulk enhance enantioselectivity, making it valuable in the synthesis of pharmaceuticals and fine chemicals where precise chirality is critical.

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid oxazoline-quinoline framework coordinates effectively with transition metals like copper or palladium, enabling high stereocontrol in reactions such as cyclopropanations, aldol additions, and allylic alkylations. The ligand’s C2-symmetry and steric bulk enhance enantioselectivity, making it valuable in the synthesis of pharmaceuticals and fine chemicals where precise chirality is critical. It is especially effective in reactions requiring mild conditions and high yield with minimal byproduct formation.

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